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Hyperbaric Oxygen Therapy for Optic Neuropathy (HBOT Trial)
N/A
Recruiting
Research Sponsored by Stanford University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Participant must be at least 18 years old
Participant with clinical evidence of optic neuropathy
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline through 6 months
Summary
This trial tests if hyperbaric oxygen therapy can help protect vision in people with optic neuropathy.
Who is the study for?
This trial is for adults over 18 with optic neuropathy, who can follow the study's schedule and understand/sign the consent form. It's not suitable for those unable to meet these requirements or participate fully.
What is being tested?
The study tests hyperbaric oxygen therapy's ability to protect nerve cells in the eye from damage caused by optic neuropathy. Participants will either receive real or sham (fake) treatments to compare effectiveness.
What are the potential side effects?
Hyperbaric oxygen therapy may cause ear pressure, temporary nearsightedness, lung collapse due to air pressure changes, and rarely, oxygen poisoning which could lead to seizures.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 18 years old or older.
Select...
I have been diagnosed with optic neuropathy.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline through 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline through 6 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in Visual Field- Mean Deviation
Change in Visual Field- Visual Field Index
Secondary study objectives
Change in Average Thickness Ganglion Cell Complex on Optical Coherence Tomography
Change in Average Thickness Retinal Nerve Fiber Layer on Optical Coherence Tomography
Trial Design
3Treatment groups
Experimental Treatment
Placebo Group
Group I: Open LabelExperimental Treatment1 Intervention
Participants will get Hyperbaric oxygen therapy for 20 days to determine best methods for full trial.
Group II: Active Hyperbaric OxygenExperimental Treatment1 Intervention
Participants will get Hyperbaric oxygen therapy for 20 days.
Group III: Sham Hyperbaric OxygenPlacebo Group1 Intervention
Participants will get a Sham Hyperbaric oxygen therapy for 20 days
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Hyperbaric Oxygen
2005
Completed Phase 3
~260
Find a Location
Who is running the clinical trial?
Stanford UniversityLead Sponsor
2,469 Previous Clinical Trials
17,501,687 Total Patients Enrolled
12 Trials studying Glaucoma
563 Patients Enrolled for Glaucoma
Jeffrey L Goldberg, MD PhDStudy ChairStanford University
2 Previous Clinical Trials
65 Total Patients Enrolled
2 Trials studying Glaucoma
65 Patients Enrolled for Glaucoma
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